E. Nelis Et Al. , "A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths," NEUROMUSCULAR DISORDERS , vol.12, no.9, pp.869-873, 2002
Nelis, E. Et Al. 2002. A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths. NEUROMUSCULAR DISORDERS , vol.12, no.9 , 869-873.
Nelis, E., Erdem, S., Tan, E., Lofgren, A., Ceuterick, C., De Jonghe, P., ... Van Broeckhoven, C.(2002). A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths. NEUROMUSCULAR DISORDERS , vol.12, no.9, 869-873.
Nelis, E Et Al. "A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths," NEUROMUSCULAR DISORDERS , vol.12, no.9, 869-873, 2002
Nelis, E Et Al. "A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths." NEUROMUSCULAR DISORDERS , vol.12, no.9, pp.869-873, 2002
Nelis, E. Et Al. (2002) . "A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths." NEUROMUSCULAR DISORDERS , vol.12, no.9, pp.869-873.
@article{article, author={E Nelis Et Al. }, title={A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths}, journal={NEUROMUSCULAR DISORDERS}, year=2002, pages={869-873} }